Medical Device Manufacturer · US , Raynham , MA

Johnson & Johnson Company - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Johnson & Johnson Company Orthopedic ✕
2 devices
1-2 of 2
Cleared Jan 25, 2007
FEMORAL INTRAFIX SCREW AND SHEATH
K063577 · MBI
Orthopedic · 56d
Cleared Jun 09, 2006
TRIDENT ANCHOR
K060914 · HWC
Orthopedic · 66d
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